Length scales in electrolytes

TL;DR

This study uses extensive Molecular Dynamics simulations to investigate electrolyte properties across concentrations, identifying a plausible origin for the experimentally observed anomalously increasing screening length at high ionic concentrations.

Contribution

The paper provides a detailed simulation-based analysis of electrolyte behavior, clarifying the origin of the long-range screening length observed in experiments, without relying on phenomenological assumptions.

Findings

Identified a candidate for the anomalously increasing screening length.

Quantified structural, dielectric, and transport changes across concentrations.

Revealed nano-scale ion organization related to the long-range effects.

Abstract

The elusive presence of an anomalously increasing screening length at high ionic concentrations hampers a complete picture of interactions in electrolytes. Theories which extend the diluted Debye-Huckel framework to higher concentrations predict, in addition to the expected decreasing Debye length, an increasing significant scale of the order of at most a few ionic diameters. More recent surface force balance experiments with different materials succeeded in measuring increasing length scales which, however, turn out to extend over tenths or even hundreds of ionic diameters. While simulation work has managed to characterize the former, the latter still avoid detection, generating doubts about its true origin. Here we provide a step forward in the clarification of such a conundrum. We have studied by extensive Molecular Dynamics simulation the properties of a generic model of electrolyte, lithium tetrafluoroborate dissolved in ethylene-carbonate, in a vast range of salt concentrations continuously joining the Debye non-interacting limit to the opposite over-charged solvent-in-salt states. On one side, we have accurately determined the macroscopic concentration-induced structural, dielectric and transport modifications, on the other we have quantified the resulting nano-scale ions organization. Based only on the simulation data, without resorting to any uncontrolled hypothesis or phenomenological parameter, we identify a convincing candidate for the measured anomalously increasing length, whose origin has been possibly misinterpreted.